Cargando…

Impact of Time to Castration Resistance on Survival in Metastatic Hormone Sensitive Prostate Cancer Patients in the Era of Combination Therapies

BACKGROUND: To evaluate the impact of time to castration resistance (TTCR) in metastatic hormone-sensitive prostate cancer (mHSPC) patients on overall survival (OS) in the era of combination therapies for mHSPC. MATERIAL AND METHODS: Of 213 mHSPC patients diagnosed between 01/2013-12/2020 who subseq...

Descripción completa

Detalles Bibliográficos
Autores principales: Wenzel, Mike, Preisser, Felix, Hoeh, Benedikt, Schroeder, Maria, Würnschimmel, Christoph, Steuber, Thomas, Heinzer, Hans, Banek, Severine, Ahrens, Marit, Becker, Andreas, Karakiewicz, Pierre I., Chun, Felix K. H., Kluth, Luis A., Mandel, Philipp
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Frontiers Media S.A. 2021
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC8103198/
https://www.ncbi.nlm.nih.gov/pubmed/33968764
http://dx.doi.org/10.3389/fonc.2021.659135
_version_ 1783689271231643648
author Wenzel, Mike
Preisser, Felix
Hoeh, Benedikt
Schroeder, Maria
Würnschimmel, Christoph
Steuber, Thomas
Heinzer, Hans
Banek, Severine
Ahrens, Marit
Becker, Andreas
Karakiewicz, Pierre I.
Chun, Felix K. H.
Kluth, Luis A.
Mandel, Philipp
author_facet Wenzel, Mike
Preisser, Felix
Hoeh, Benedikt
Schroeder, Maria
Würnschimmel, Christoph
Steuber, Thomas
Heinzer, Hans
Banek, Severine
Ahrens, Marit
Becker, Andreas
Karakiewicz, Pierre I.
Chun, Felix K. H.
Kluth, Luis A.
Mandel, Philipp
author_sort Wenzel, Mike
collection PubMed
description BACKGROUND: To evaluate the impact of time to castration resistance (TTCR) in metastatic hormone-sensitive prostate cancer (mHSPC) patients on overall survival (OS) in the era of combination therapies for mHSPC. MATERIAL AND METHODS: Of 213 mHSPC patients diagnosed between 01/2013-12/2020 who subsequently developed metastatic castration resistant prostate cancer (mCRPC), 204 eligible patients were analyzed after having applied exclusion criteria. mHSPC patients were classified into TTCR <12, 12-18, 18-24, and >24 months and analyzed regarding OS. Moreover, further OS analyses were performed after having developed mCRPC status according to TTCR. Logistic regression models predicted the value of TTCR on OS. RESULTS: Median follow-up was 34 months. Among 204 mHSPC patients, 41.2% harbored TTCR <12 months, 18.1% for 12-18 months, 15.2% for 18-24 months, and 25.5% for >24 months. Median age was 67 years and median PSA at prostate cancer diagnosis was 61 ng/ml. No differences in patient characteristics were observed (all p>0.05). According to OS, TTCR <12 months patients had the worst OS, followed by TTCR 12-18 months, 18-24 months, and >24 months, in that order (p<0.001). After multivariable adjustment, a 4.07-, 3.31-, and 6.40-fold higher mortality was observed for TTCR 18-24 months, 12-18 months, and <12 months patients, relative to TTCR >24 months (all p<0.05). Conversely, OS after development of mCRPC was not influenced by TTCR stratification (all p>0.05). CONCLUSION: Patients with TTCR <12 months are at the highest OS disadvantage in mHSPC. This OS disadvantage persisted even after multivariable adjustment. Interestingly, TTCR stratified analyses did not influence OS in mCRPC patients.
format Online
Article
Text
id pubmed-8103198
institution National Center for Biotechnology Information
language English
publishDate 2021
publisher Frontiers Media S.A.
record_format MEDLINE/PubMed
spelling pubmed-81031982021-05-08 Impact of Time to Castration Resistance on Survival in Metastatic Hormone Sensitive Prostate Cancer Patients in the Era of Combination Therapies Wenzel, Mike Preisser, Felix Hoeh, Benedikt Schroeder, Maria Würnschimmel, Christoph Steuber, Thomas Heinzer, Hans Banek, Severine Ahrens, Marit Becker, Andreas Karakiewicz, Pierre I. Chun, Felix K. H. Kluth, Luis A. Mandel, Philipp Front Oncol Oncology BACKGROUND: To evaluate the impact of time to castration resistance (TTCR) in metastatic hormone-sensitive prostate cancer (mHSPC) patients on overall survival (OS) in the era of combination therapies for mHSPC. MATERIAL AND METHODS: Of 213 mHSPC patients diagnosed between 01/2013-12/2020 who subsequently developed metastatic castration resistant prostate cancer (mCRPC), 204 eligible patients were analyzed after having applied exclusion criteria. mHSPC patients were classified into TTCR <12, 12-18, 18-24, and >24 months and analyzed regarding OS. Moreover, further OS analyses were performed after having developed mCRPC status according to TTCR. Logistic regression models predicted the value of TTCR on OS. RESULTS: Median follow-up was 34 months. Among 204 mHSPC patients, 41.2% harbored TTCR <12 months, 18.1% for 12-18 months, 15.2% for 18-24 months, and 25.5% for >24 months. Median age was 67 years and median PSA at prostate cancer diagnosis was 61 ng/ml. No differences in patient characteristics were observed (all p>0.05). According to OS, TTCR <12 months patients had the worst OS, followed by TTCR 12-18 months, 18-24 months, and >24 months, in that order (p<0.001). After multivariable adjustment, a 4.07-, 3.31-, and 6.40-fold higher mortality was observed for TTCR 18-24 months, 12-18 months, and <12 months patients, relative to TTCR >24 months (all p<0.05). Conversely, OS after development of mCRPC was not influenced by TTCR stratification (all p>0.05). CONCLUSION: Patients with TTCR <12 months are at the highest OS disadvantage in mHSPC. This OS disadvantage persisted even after multivariable adjustment. Interestingly, TTCR stratified analyses did not influence OS in mCRPC patients. Frontiers Media S.A. 2021-04-23 /pmc/articles/PMC8103198/ /pubmed/33968764 http://dx.doi.org/10.3389/fonc.2021.659135 Text en Copyright © 2021 Wenzel, Preisser, Hoeh, Schroeder, Würnschimmel, Steuber, Heinzer, Banek, Ahrens, Becker, Karakiewicz, Chun, Kluth and Mandel https://creativecommons.org/licenses/by/4.0/This is an open-access article distributed under the terms of the Creative Commons Attribution License (CC BY). The use, distribution or reproduction in other forums is permitted, provided the original author(s) and the copyright owner(s) are credited and that the original publication in this journal is cited, in accordance with accepted academic practice. No use, distribution or reproduction is permitted which does not comply with these terms.
spellingShingle Oncology
Wenzel, Mike
Preisser, Felix
Hoeh, Benedikt
Schroeder, Maria
Würnschimmel, Christoph
Steuber, Thomas
Heinzer, Hans
Banek, Severine
Ahrens, Marit
Becker, Andreas
Karakiewicz, Pierre I.
Chun, Felix K. H.
Kluth, Luis A.
Mandel, Philipp
Impact of Time to Castration Resistance on Survival in Metastatic Hormone Sensitive Prostate Cancer Patients in the Era of Combination Therapies
title Impact of Time to Castration Resistance on Survival in Metastatic Hormone Sensitive Prostate Cancer Patients in the Era of Combination Therapies
title_full Impact of Time to Castration Resistance on Survival in Metastatic Hormone Sensitive Prostate Cancer Patients in the Era of Combination Therapies
title_fullStr Impact of Time to Castration Resistance on Survival in Metastatic Hormone Sensitive Prostate Cancer Patients in the Era of Combination Therapies
title_full_unstemmed Impact of Time to Castration Resistance on Survival in Metastatic Hormone Sensitive Prostate Cancer Patients in the Era of Combination Therapies
title_short Impact of Time to Castration Resistance on Survival in Metastatic Hormone Sensitive Prostate Cancer Patients in the Era of Combination Therapies
title_sort impact of time to castration resistance on survival in metastatic hormone sensitive prostate cancer patients in the era of combination therapies
topic Oncology
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC8103198/
https://www.ncbi.nlm.nih.gov/pubmed/33968764
http://dx.doi.org/10.3389/fonc.2021.659135
work_keys_str_mv AT wenzelmike impactoftimetocastrationresistanceonsurvivalinmetastatichormonesensitiveprostatecancerpatientsintheeraofcombinationtherapies
AT preisserfelix impactoftimetocastrationresistanceonsurvivalinmetastatichormonesensitiveprostatecancerpatientsintheeraofcombinationtherapies
AT hoehbenedikt impactoftimetocastrationresistanceonsurvivalinmetastatichormonesensitiveprostatecancerpatientsintheeraofcombinationtherapies
AT schroedermaria impactoftimetocastrationresistanceonsurvivalinmetastatichormonesensitiveprostatecancerpatientsintheeraofcombinationtherapies
AT wurnschimmelchristoph impactoftimetocastrationresistanceonsurvivalinmetastatichormonesensitiveprostatecancerpatientsintheeraofcombinationtherapies
AT steuberthomas impactoftimetocastrationresistanceonsurvivalinmetastatichormonesensitiveprostatecancerpatientsintheeraofcombinationtherapies
AT heinzerhans impactoftimetocastrationresistanceonsurvivalinmetastatichormonesensitiveprostatecancerpatientsintheeraofcombinationtherapies
AT banekseverine impactoftimetocastrationresistanceonsurvivalinmetastatichormonesensitiveprostatecancerpatientsintheeraofcombinationtherapies
AT ahrensmarit impactoftimetocastrationresistanceonsurvivalinmetastatichormonesensitiveprostatecancerpatientsintheeraofcombinationtherapies
AT beckerandreas impactoftimetocastrationresistanceonsurvivalinmetastatichormonesensitiveprostatecancerpatientsintheeraofcombinationtherapies
AT karakiewiczpierrei impactoftimetocastrationresistanceonsurvivalinmetastatichormonesensitiveprostatecancerpatientsintheeraofcombinationtherapies
AT chunfelixkh impactoftimetocastrationresistanceonsurvivalinmetastatichormonesensitiveprostatecancerpatientsintheeraofcombinationtherapies
AT kluthluisa impactoftimetocastrationresistanceonsurvivalinmetastatichormonesensitiveprostatecancerpatientsintheeraofcombinationtherapies
AT mandelphilipp impactoftimetocastrationresistanceonsurvivalinmetastatichormonesensitiveprostatecancerpatientsintheeraofcombinationtherapies